نمایش مختصر رکورد

dc.date.accessioned1399-07-08T17:55:29Zfa_IR
dc.date.accessioned2020-09-29T17:55:29Z
dc.date.available1399-07-08T17:55:29Zfa_IR
dc.date.available2020-09-29T17:55:29Z
dc.date.issued2012-03-01en_US
dc.date.issued1390-12-11fa_IR
dc.identifier.citation(2012). Knockdown of Radixin by RNA Interference Suppresses the Growth of Human Pancreatic Cancer Cells in Vitro and in Vivo. Asian Pacific Journal of Cancer Prevention, 13(3), 753-759.en_US
dc.identifier.issn1513-7368
dc.identifier.issn2476-762X
dc.identifier.urihttp://journal.waocp.org/article_26216.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/32271
dc.description.abstractRadixin, encoded by a gene on chromosome 11, plays important roles in cell motility, invasion and tumor progression. However, its function in pancreatic cancer remains elusive. In this study, radixin gene expression was suppressed with a lentivirus-mediated short-hairpin RNA (shRNA) method. We found that radixin shRNA caused down-regulation of radixin in PANC-1 cells, associated with inhibition of pancreatic cancer cell proliferation, survival, adhesion and invasive potential in vitro. When radixin-silenced cells were implanted in nude mice, tumor growth and microvessel density were significantly inhibited as compared to blank control cells or nonsense shRNA control cells. Thrombospondin-1 (TSP-1) and E-cadherin were up-regulated in radixin-silenced PANC-1 cells. Our results suggest that radixin might play a critical role in pancreatic cancer progression, possibly through invvolvement of down-regulation of TSP-1 and E-cadherin expression.en_US
dc.format.extent1311
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherWest Asia Organization for Cancer Prevention (WAOCP)en_US
dc.relation.ispartofAsian Pacific Journal of Cancer Preventionen_US
dc.subjectPancreatic neoplasmsen_US
dc.subjectsmall interference RNAen_US
dc.subjectradixinen_US
dc.titleKnockdown of Radixin by RNA Interference Suppresses the Growth of Human Pancreatic Cancer Cells in Vitro and in Vivoen_US
dc.typeTexten_US
dc.citation.volume13
dc.citation.issue3
dc.citation.spage753
dc.citation.epage759


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